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Maria-Elena Torres-PadillaView profile

Professor

• Epigenetics
• Stem Cell Biology
• Early Mammalian Development
• +6 more

Maria-Elena Torres-Padilla is a Director at the Helmholtz Centre Munich and Full Professor (W3) for Stem Cell Biology at the Ludwig-Maximilians University, Munich . She leads the Institute of Epigenetics & Stem Cells and the Stem Cell Centre , with affiliations to the Helmholtz Pioneer Campus and IGBMC, Strasbourg . Education : Habilitation in Molecular & Cellular Biology (2008, Université Louis Pasteur); PhD in Molecular & Cellular Biology (1998–2002, Université Paris V/Institut Pasteur); University degree in Biology (1994–1998, National University of Mexico). Research Interests focus on epigenetics , chromatin dynamics , stem cell biology , and early mammalian development . Her work explores nuclear organization, totipotency, and reprogramming mechanisms during embryogenesis, with a strong emphasis on histone variants, heterochromatin regulation, and 3D genome architecture. Her publications span high-impact journals like Nature , Nature Cell Biology , and Nature Genetics , with a focus on epigenetic reprogramming, chromatin accessibility, and cell fate decisions. She has authored 84 publications, including 62 as first or corresponding author. Scientific Awards & Leadership Roles : 2023: Member, German National Academy of Sciences (Leopoldina) and Latin American Academy of Sciences (ACAL) 2021–2023: Editorial Board Member, Science and Cell Stem Cell 2020: NIH 4D Nucleome Project Principal Investigator Award 2019–2021: Founding member and Work Package Leader, LifeTime Initiative 2018–2023: Steering Board Member, Single Cell Omics Germany She actively participates in interdisciplinary networks , including EpiGeneSys , Helmholtz Think Tank , and NIH 4D Nucleome advisory roles, while organizing major conferences like the Gordon Research Conference on Epigenetics and FASEB Methylation Meetings .

Jae Young ChoiView profile

Assistant Professor

• Evolutionary Genomics
• Adaptive Radiation
• Telomere Evolution
• +3 more

Dr. Jae Young Choi is an Assistant Professor in the Department of Ecology and Evolutionary Biology at the University of Kansas. His research focuses on evolutionary genomics, adaptive radiation, and telomere evolution, using plants as model systems. He integrates genomic technologies with field and lab phenotypic data to study evolutionary mechanisms driving biodiversity. Education: B.S. in Cell and Systems Biology (University of Toronto, 2010), Ph.D. in Population Genetics (Cornell University, 2015). Research interests include plant adaptation through genomic analysis, telomere biology, and domestication history. The lab develops tools like Topsicle for telomere length estimation using long-read sequencing. Recent grants include an NIH R35 Award for telomere variation studies. Advising involves graduate students (e.g., Surbhi, Khan, Linh) and undergraduate researchers (Audrey). The lab actively participates in conferences like MWPG2024 and publishes in journals like PNAS , Plant Cell , and Molecular Biology and Evolution . Labs/Teams: Choi Lab at KU, focusing on evolutionary genomics and computational tools development.

• Genetics
• Functional Genomics
• Neurodevelopmental Disorders
• +12 more

Kristina Lanko is an Assistant Professor in the Department of Clinical Genetics at Erasmus MC, Faculty of Medicine. Her research is centered on understanding the genetic and molecular basis of neurodevelopmental and neurodegenerative disorders, with a strong focus on functional genomics and gene regulation. Her research interests span Genetics , Neuronal Differentiation , Regulatory Elements , Non-coding DNA , and Neurodevelopmental Disorders . She employs in vitro models, zebrafish, and patient-derived cells to study disease mechanisms and identify potential therapeutic strategies. Her work integrates molecular biology, epigenetics, and computational approaches to interpret disease-relevant genetic variants. The most recent articles highlight a consistent focus on neurogenetics and translational genomics . Themes include the role of ubiquitin proteases in neurodevelopment (e.g., USP7), modeling hereditary spastic paraplegia, interpreting non-coding variants using AI, and identifying biomarkers for spinal muscular atrophy. These studies demonstrate a translational trajectory from basic molecular mechanisms to clinical applications. No scientific awards were mentioned in the provided text. Kristina Lanko actively collaborates with leading researchers in the field, including Dr. Tamer Barakat, and contributes to significant discoveries in rare genetic diseases. While specific grants or advising roles are not detailed, her position as an assistant professor and co-authorship on multiple high-impact papers suggest active mentorship and research leadership. Her work is published in top-tier journals such as Genes & Development , Acta Neuropathologica , and Journal of Neuroinflammation . She is involved in building functional genomics resources and preclinical models, indicating leadership in a research team or lab focused on precision medicine for neurological disorders.

• Animal genetics
• Molecular biology
• Stress response
• +4 more

Eduard Muráni is a Researcher at the Leibniz Institute for Farm Animal Biology (FBN) in Dummerstorf, Germany, where he leads the Physiological Genomics working group. He holds a Ph.D. in Agricultural Science from the University of Bonn and an MSc from Constantine the Philosopher University in Slovakia. Muráni's research focuses on the molecular biology and genetics of traits related to production, adaptation, and welfare in pigs , with particular emphasis on stress response, behavior, and muscle development . His work explores how mRNA expression regulation connects genetic variation with phenotypic outcomes. Recent publications highlight his contributions to understanding glucocorticoid receptor hypersensitivity , phosphorus utilization , stress-induced gene expression changes , and immune-metabolic interactions in pigs. His studies employ transcriptomics, epigenetics, and functional genomics approaches to investigate gene-environment interactions across multiple physiological systems .

Ioannis PolitisView profile

Professor

• Nutritional Physiology
• Lactation Physiology
• Dairy Science
• +7 more

Ioannis Politis is a Professor of Nutritional Physiology and Performance of Farm Animals at the Agricultural University of Athens. He served as Chair of the Department of Animal Production and Aquaculture Science (2011-2015) and Dean of the School of Agricultural Production, Infrastructure and Environment (2015-2018). He holds a Ph.D. from McGill University (Canada) and has held academic positions at the University of Guelph, Cornell University, and the University of Vermont in the US before joining AUA. Education: Ph.D. in Animal Science, McGill University, Canada (1989) Postdoctoral Researcher: University of Guelph (1989-1990), Cornell University (1990-1993) Assistant Professor (Tenured Track): University of Vermont (1993-1996) Research Focus: Interactions between nutrition and immune function in livestock Identification of bioactive milk peptides with antihypertensive and immunomodulatory properties Plasminogen activator system and its role in mammary gland physiology Optimization of dairy byproduct utilization in animal feed and functional foods Recent Article Trends: His recent work emphasizes valorization of dairy byproducts (e.g., whey), exploration of immunomodulatory peptides, and sustainable agricultural practices through agro-industrial waste utilization. Key themes include enhancing animal health through diet optimization and developing functional foods from biological waste streams. Labs & Affiliations: Directs the Laboratory of Animal Breeding & Husbandry and collaborates with the Nutrition & Diet Physiology Laboratory. His research integrates animal physiology, microbiology, and food science to address challenges in livestock productivity and human nutrition.

Olivia CorradinView profile

Professor

• Genetic and epigenetic regulation
• Gene regulatory elements in disease
• Multiple Sclerosis
• +3 more

Olivia Corradin is the Class of 1922 Career Development Professor in MIT's Department of Biology and a Core Member of the Whitehead Institute for Biomedical Research. Her research focuses on genetic and epigenetic mechanisms underlying human diseases, particularly Multiple Sclerosis and Opioid Use Disorder. She earned her PhD in 2015 from Case Western Reserve University and a BS in Biochemistry from Marquette University (2010). Her lab investigates how genetic variants in regulatory elements disrupt gene expression programs, combining multi-omic approaches to study disease risk. Notable contributions include identifying oligodendrocyte mechanisms in MS and uncovering epigenetic vulnerabilities in opioid addiction. Awarded the NIH Pioneer Award (2017), her work bridges basic science and clinical applications. Current projects include CRISPR-based screening to dissect disease pathways and understanding microglial roles in neurodegenerative disorders. Lab members include PhD students Yasmine Sami (Biology, MIT) and Chesna Apere (Neuroscience), postdoc Pavana Rotti (epigenetics), and data scientists An Hoang and Fatir Qureshi. Collaborations span computational biology, stem cell models, and post-mortem tissue analysis.

• Molecular Cancer Biology
• Melanoma Metastasis
• Immunotherapy Resistance
• +7 more

Jean-Christophe Marine is a full professor at the KU Leuven Faculty of Medicine , leading the Laboratory for Molecular Cancer Biology (VIB-KU Leuven). His work focuses on unraveling molecular mechanisms in melanoma and pancreatic cancer, with a particular emphasis on metastasis, immunotherapy resistance, and tumor microenvironment dynamics. Head, Laboratory for Molecular Cancer Biology (VIB-KU Leuven) Head, VIB-KU Leuven Center for Cancer Biology - Administrative Core Member, VIB-KU Leuven Center for Cancer Biology Member, LISCO - KU Leuven Institute for Single Cell Omics Senior academic staff, Faculty of Medicine Council His research spans cell state plasticity , lipid metabolism in metastasis , epitranscriptomic regulation , and novel spatial analysis technologies . Recent projects include studying extracellular vesicles in pre-metastatic niche formation and developing AI-driven pipelines for cancer cell mapping. Publications highlight discoveries in NK cell-mediated immunotherapy resistance , alternative translation in metastasis , and oncofetal reprogramming in colorectal cancer. Collaborative work includes defining stromal lipid species as metastatic drivers and mapping melanoma subclone plasticity using single-cell multi-omics. Current affiliations include leadership roles in cancer biology centers and advisory positions in institutional councils. His work intersects basic research and clinical translation , with major implications for precision oncology.

• Cardiovascular Development
• Stem Cell Biology
• Genomics
• +2 more

Ian McCracken is an MRC Transition Fellow at the Department of Physiology, Anatomy and Genetics (DPAG), University of Oxford, working within Dr. Nicola Smart's research group. His research focuses on elucidating molecular mechanisms controlling cardiovascular development, particularly transcriptional regulation of endothelial and endocardial cell differentiation. His academic background includes: Undergraduate degree in Biomedical Sciences from Royal Holloway, University of London PhD from the University of Edinburgh under the MRC Precision Medicine Doctoral Training Programme, supervised by Prof Andy Baker and Prof Chris Ponting McCracken's research integrates single-cell RNA sequencing with human pluripotent stem cell differentiation models to investigate transcriptional landscapes during cardiac development. His current work examines endocardial plasticity mechanisms using in vivo and hiPSC-based in vitro approaches, aiming to identify therapeutic targets for heart regeneration following cardiovascular injury. This bridges developmental biology with regenerative medicine applications. His 2024 preprint on arterial enhancers demonstrates expertise in genomic regulation of vascular development, representing ongoing contributions to cardiovascular genomics. Key recognition: MRC Transition Fellowship (2020) Funded by his MRC Transition Fellowship, McCracken leads independent research within Dr. Smart's group at DPAG, leveraging interdisciplinary collaborations to study endocardial-to-coronary endothelial cell transitions. The department's #1 QS World Ranking in Anatomy & Physiology provides an exceptional environment for his cardiovascular developmental biology investigations.

Sherif El-KhamisyView profile

Professor

• DNA Repair
• Genomic Instability
• Neurodegenerative Diseases
• +17 more

Sherif El-Khamisy is Professor of Molecular Medicine in the School of Biosciences at the University of Sheffield , where he also serves as Deputy Director of the Healthy Lifespan Institute. He leads an active research group investigating DNA repair mechanisms and their roles in neurodegeneration and cancer. His lab is affiliated with the Neuroscience Institute and collaborates widely across clinical and translational research domains. Education and Career El-Khamisy earned his PhD in Biochemistry from the University of Sussex (2002–2005). He held postdoctoral positions at St Jude Children’s Research Hospital (USA) and the University of Sussex, before joining the University of Sheffield in 2008. He has held continuous academic leadership roles, including Chair of Molecular Medicine and Wellcome Trust Investigator. Research Interests His research focuses on DNA repair , particularly the repair of topoisomerase-mediated and oxidative DNA damage, and its implications in neurodegenerative diseases (e.g., ALS, Huntington’s, ataxias) and cancer . His lab explores mitochondrial DNA repair, R-loops, transcription-coupled repair, and genomic instability in stem cells and aging. He integrates genetics, biochemistry, and clinical insights to uncover novel pathways and therapeutic strategies. Publication Trends His recent work (2022–2025) emphasizes oxidative DNA damage in regulatory regions, glucose-induced genotoxicity, cancer-specific glycosylation, and mechanisms of chemotherapy resistance. There is a strong focus on translational applications, including nanomedicine, biomarker discovery, and personalized therapy, often using zebrafish and human cell models. Scientific Awards and Honors Wellcome Trust Investigator Award Lister Research Fellow Fellow of the Royal Society of Chemistry Fellow of the Royal Society of Biology Fellow of the Lister Institute of Preventative Medicine Shoman Award for Medical Sciences Sir Richard Stapley Award, UK Lorne Duncan Award, UK Advising and Grants El-Khamisy actively mentors PhD and postdoctoral researchers, with former students establishing independent careers. His group has received funding from the Wellcome Trust, Lister Institute, and collaborations with AstraZeneca and CRUK. He has led drug discovery initiatives and developed novel genomic technologies with clinical applications. Labs and Teams He leads the El-Khamisy Lab , which investigates DNA repair in disease models. The lab has developed zebrafish models, conducted drug screens with Artios Pharma, and collaborated with industry on diagnostic tools. The team includes postdocs, PhD students, and clinical fellows working on neurodegeneration, cancer, and stem cell genomics.

Jeanne B LawrenceView profile

Professor

• Epigenetics
• Chromosome Organization
• Non-coding RNA
• +5 more

Jeanne B Lawrence is the Leo P. and Theresa M. LaChance Chair in Medical Research and Professor of Neurology and Pediatrics at the University of Massachusetts Chan Medical School. She has been a faculty member at UMass Chan since 1985, following her PhD in developmental biology from Brown University in 1982. Her groundbreaking work has established fundamental principles in chromosome biology and epigenetics. Dr. Lawrence's research focuses on nuclear and genome organization, particularly the role of non-coding RNA in chromosome regulation. Her lab pioneered techniques to visualize individual genes and RNAs within nuclear structure, leading to the seminal discovery that XIST RNA coats the inactive X-chromosome and induces epigenetic silencing. Her work has revealed how large-scale segmental genome architecture relates to cytogenetic bands and repeat elements, demonstrating that repeat-rich RNAs play critical structural roles in maintaining open chromatin packaging. Her lab has made several major discoveries: (1) XIST RNA's capacity to silence an entire chromosome, (2) the structural role of repeat-rich RNAs in chromosome architecture, (3) the link between satellite II repeats and cancer-specific nuclear bodies, and (4) the application of XIST technology to silence trisomy 21 in Down syndrome patient stem cells. Her recent work examines how Alu and L1 repeats distribute after X-chromosome inactivation and how they relate to chromatin regulation. Analysis of Dr. Lawrence's publications reveals consistent focus on chromosome architecture and non-coding RNA function. Her work spans fundamental mechanisms of X-chromosome inactivation, the structural role of repeat elements in genome organization, and translational applications for chromosomal disorders. The publications demonstrate evolution from early cytological studies to modern transcriptomic and biochemical approaches, with increasing emphasis on repeat elements and their roles in both normal development and disease. Dr. Lawrence's research has been continuously funded through competitive grants, enabling her lab to develop innovative technologies like stringent biochemical fractionation and RNAseq transcriptomics. Her work bridges fundamental chromosome biology with clinical applications, particularly in developing approaches to correct chromosomal abnormalities like Down syndrome through epigenetic silencing. The Lawrence Lab maintains active research programs in nuclear architecture, X-chromosome inactivation mechanisms, repeat genome function, and translational applications for chromosomal disorders. The lab utilizes advanced molecular cytology, biochemical fractionation, and genomic approaches to investigate how large-scale chromosome organization relates to gene regulation in development and disease.

Alexander Francis PalazzoView profile

Professor

• Molecular Biology
• Cell Biology
• RNA Biology
• +3 more

Dr. Alexander F. Palazzo is a Professor in the Department of Biochemistry at the University of Toronto's Faculty of Medicine. His research focuses on the mechanisms governing mRNA nuclear export, subcellular localization, and the evolutionary forces shaping genomic nucleotide content. He has made significant contributions to understanding how cells distinguish functional RNAs from non-coding transcripts, and how RNA localization influences protein synthesis in specific cellular compartments. PhD in Cell Biology (Columbia University) Postdoctoral Fellowship at Harvard Medical School Dr. Palazzo's work integrates cell biology, biochemistry, and computational approaches to investigate: mRNA export through nuclear pores ER-targeted translation mechanisms Evolutionary patterns in gene structure Role of nuclear pore proteins in disease His publications reveal trends in RNA processing, disease mechanisms in Acute Necrotizing Encephalopathy, and evolutionary origins of functional elements from non-coding DNA. Awards include the Ontario Early Researcher Award, CIHR New Investigator Award, and multiple teaching distinctions. Jean D'Alembert Chair (2023-2024) Mid-Career Excellence in Graduate Teaching (2020) Connaught New Researcher Award (2011) Dr. Palazzo teaches graduate courses in evolutionary thinking and interdisciplinary science, and leads a multidisciplinary lab combining experimental and computational approaches to study RNA biogenesis and cellular information processing.

Joshua D WytheView profile

Associate Professor

• Cardiovascular Biology
• Cerebrovascular Pathologies
• Developmental Biology
• +12 more

Joshua D. Wythe is an Associate Professor in the Department of Cell and Developmental Biology at the University of Virginia School of Medicine. His research focuses on the molecular and genetic mechanisms underlying cardiovascular development and cerebrovascular pathologies, with a particular emphasis on endothelial cell differentiation and brain vascular diseases such as arteriovenous malformations and glioblastoma. He leads the Wythe Lab, which utilizes zebrafish and mouse models combined with bioinformatics, functional genomics, and 3D imaging to investigate blood vessel formation and dysfunction. BA in History, Miami University BS in Botany, Miami University PhD in Oncological Sciences / Cardiovascular Development, University of Utah School of Medicine Postdoctoral Fellowship in Cardiovascular Development and Disease, University of California, San Francisco Dr. Wythe's research interests span cardiovascular biology, developmental biology, transcriptional regulation, and translational science. His lab investigates how transcriptional networks govern endothelial plasticity, the role of RAS/MEK/ERK signaling in brain arteriovenous malformations, and novel therapeutic targets in glioblastoma. The work integrates molecular genetics, imaging, and bioinformatics to understand both normal vascular development and pathological conditions. The recent publications reflect a strong trend in vascular development, disease modeling, and technological innovation. Key themes include transcriptional control of endothelial identity, signaling pathways in vascular malformations, and advanced imaging techniques for 3D tissue visualization. The research spans from basic developmental mechanisms to translational applications in brain cancers and cerebrovascular disorders. Dr. Wythe actively mentors graduate students, postdoctoral fellows, and undergraduates, fostering a collaborative and interdisciplinary research environment. His lab is currently recruiting researchers with expertise in developmental biology, genomics, bioinformatics, and imaging. Funding supports multiple projects aimed at uncovering transcriptional regulators essential for cardiovascular function and disease. The Wythe Lab is equipped to conduct cutting-edge research using genetically modified animal models, single-cell analyses, and advanced microscopy. The team develops and shares resources such as FishNET for zebrafish colony management and EZ Clear for tissue clearing, contributing to the broader scientific community.

Francisco J. Ruiz-RuanoView profile

Research Fellow

• Evolutionary Genetics
• Genome Architecture
• Cytogenetics
• +6 more

Francisco J. Ruiz-Ruano is a Postdoctoral Researcher at the School of Biological Sciences, University of East Anglia (UEA), actively engaged in research on genome evolution and molecular genetics. His work bridges cytogenetics and genomics, focusing on non-model organisms such as birds, insects, fish, and ferns. His research interests lie at the intersection of evolutionary genetics , genome architecture , and molecular cytogenetics . He investigates the role of repetitive DNA elements—including satellite DNA and transposable elements—in shaping genome structure and function across diverse taxa. A significant portion of his recent work explores the enigmatic germline-restricted chromosomes in songbirds, revealing non-Mendelian inheritance patterns and their evolutionary implications. The recent publication trends highlight a strong focus on comparative genomics and genome plasticity , with studies spanning avian, insect, plant, and fish systems. These works employ cutting-edge sequencing and bioinformatic tools to uncover evolutionary dynamics of repetitive DNA, offering insights into long-term genome evolution and adaptation. Francisco collaborates extensively with international researchers, as evidenced by co-authorship with teams in Spain, Germany, Brazil, and Sweden. While no formal awards are listed, his publications appear in high-impact journals such as PNAS and BMC Biology , indicating strong peer recognition. He is involved in collaborative research projects that likely involve grants from research councils or institutions, though specific funding sources are not mentioned. His work contributes significantly to understanding genome diversity and evolutionary mechanisms in non-traditional model species. He is part of an active research network within the School of Biological Sciences at UEA, contributing to genomics and evolutionary biology research. His ORCID profile (0000-0002-5391-301X) provides a comprehensive record of his scholarly output and collaborations.

• Evolutionary Developmental Biology
• Genetics
• Vertebrate Evolution
• +7 more

Tetsuya Nakamura is an Assistant Professor in the Department of Genetics at Rutgers University, School of Arts and Sciences. His research lies at the intersection of evolutionary biology, developmental genetics, and comparative anatomy, focusing on the genetic underpinnings of fish diversity and the evolutionary transition from fish to tetrapods. B.S., Bioengineering, Osaka University (2002) Ph.D., Developmental Biology, Osaka University (2007) Postdoctoral Scholar, Osaka University (2007–2008) Assistant Professor, Osaka University (2008–2012) Postdoctoral Scholar, University of Chicago (2012–2017) Assistant Professor, Rutgers University (2018–present) Dr. Nakamura's research integrates functional genomics, experimental embryology, and paleontology to uncover the developmental mechanisms behind major evolutionary innovations in vertebrates. His work emphasizes the homology between fish fins and tetrapod limbs, exploring conserved genetic programs and regulatory elements that drive morphological change across deep evolutionary time. His recent publications reveal a strong focus on the evolution of paired appendages, enhancer conservation, and the developmental basis of left-right asymmetry. Using both model and non-model organisms, his lab leverages cutting-edge genomic and imaging technologies to investigate ancient evolutionary transitions, particularly the origin of limbs and the skate genome’s insights into vertebrate phylogeny. Dr. Nakamura has not been mentioned to have received specific scientific awards in the provided text. He advises a diverse team of students and researchers at Rutgers, including Caroline Schwaner, Sayoni Chatterjee, Giaminh Ben Phan, Meghana Miryala, Elaina Legere, Tristan Alder, Hitesha Hatta, and Aashi Rana. There is no mention of external grants, but his ongoing research and lab activities suggest active funding. His lab contributes significantly to international genomics consortia and publishes in high-impact journals. Dr. Nakamura leads an active research laboratory at Rutgers University focused on evolutionary developmental biology. The lab investigates the genetic basis of fin diversity and the fish-to-tetrapod transition, combining experimental approaches with comparative genomics and paleontological data. The team includes graduate students and researchers engaged in cutting-edge studies of vertebrate evolution.

Neena GroverView profile

Professor

• RNA Biochemistry
• Nucleic Acid Biochemistry
• RNA Thermodynamics
• +3 more

Neena Grover is a Professor of RNA Biochemistry in the Chemistry & Biochemistry Department at Colorado College. She leads The Grover Lab, where she conducts research on RNA thermodynamics with undergraduate students. Her work focuses on understanding small RNA structural motifs and the role of magnesium ions in stabilizing RNA structures. As an educator, she teaches a range of courses from introductory organic chemistry to specialized topics in RNA and nucleic acid biochemistry, including courses on coronaviruses and HIV-1. Professor Grover's research interests span RNA biochemistry, nucleic acid thermodynamics, and science education. Her laboratory investigates the sequence requirements and stability of small RNA loop regions, particularly examining how metal ions contribute to RNA structure formation and function. She also explores pedagogical approaches including student-centered teaching, problem-based service learning, and anti-racist teaching methodologies. Her work bridges fundamental RNA research with practical applications, including potential contributions to understanding viral RNA structures like those in coronaviruses. Dr. Grover's scholarly output demonstrates a dual focus on RNA biochemistry and science education. Her recent publications cover thermodynamic studies of various RNA structures while also addressing cultural structures in biology education and inclusive teaching practices. This combination reflects her commitment to both advancing scientific knowledge and improving how science is taught and experienced by diverse student populations. Among her professional recognitions, Dr. Grover serves as Editor of CourseSource, an evidence-based undergraduate teaching resource for the American Society for Biochemistry and Molecular Biology (2016-present), and as an Editorial Board Member for Biochemistry and Molecular Biology Education. Her 2011 work was highlighted in the CUR Undergraduate Research Highlights. Professor Grover actively mentors undergraduate researchers, with recent students including Piper Catlin, Quinn Eaheart, Abbott Gifford, Adrian Larkspur, and Abe Rosenthal. Many of her publications feature undergraduate co-authors, demonstrating her commitment to involving students in meaningful research. She founded and advises the Student Club for Science Outreach (CC Science Outreach), extending her educational impact beyond the classroom through community engagement and science communication initiatives. The Grover Lab utilizes multiple biophysical techniques including thermal denaturation, isothermal calorimetry, fluorescence spectroscopy, and native PAGE to characterize RNA structures. The lab is expanding its capabilities with circular dichroism and Raman spectroscopy. Current research includes projects related to coronavirus RNA structures and potential RNA-based inhibitors, connecting fundamental research to contemporary health challenges while training the next generation of scientists.